Colon Cancer: Gene >> PBK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301905
Start	27823134:27823134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224G>A
AA Mutation	p.Arg75Gln(p.R75Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301905
Start	27833079:27833079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.35A>G
AA Mutation	p.Lys12Arg(p.K12R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301905
Start	27823186:27823186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172C>A
AA Mutation	p.His58Asn(p.H58N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301905
Start	27822468:27822468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.316G>A
AA Mutation	p.Ala106Thr(p.A106T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301905
Start	27810374:27810374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.900C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PBK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301905
Start	27823093:27823093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.265T>G
AA Mutation	p.Leu89Val(p.L89V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript